Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003126.2 | 7239 | Missense Mutation | CCA,TCA | P2382S | NP_003117.2 |
XM_011509916.2 | 7239 | Missense Mutation | CCA,TCA | P2382S | XP_011508218.1 |
XM_011509917.2 | 7239 | Missense Mutation | CCA,TCA | P2376S | XP_011508219.1 |
XM_011509918.2 | 7239 | Intron | XP_011508220.1 | ||
XM_011509919.2 | 7239 | Intron | XP_011508221.1 |